Second Genome

Last updated
Second Genome
Founded2010  OOjs UI icon edit-ltr-progressive.svg
Founder
  • Corey Goodman
  • Todd DeSantis
Headquarters,
United States  OOjs UI icon edit-ltr-progressive.svg
Key people
Peter DiLaura (President, CEO as of 2016)
Number of employees
25 (2016)
Website www.secondgenome.com   OOjs UI icon edit-ltr-progressive.svg

Second Genome is a venture capital funded, life sciences research company based in South San Francisco. [1] The company's focus is on the development and exploitation of a research platform which facilitates the identification and elucidation of relationships between human physiology and the human microbiota, [1] [2] and it has a long term goal of becoming a drug development company. [3] The name "second genome" comes from the notion that humans have, effectively, two genomes: the native human genome, and the more diverse set of genomes carried by the human microbiota. [4]

Contents

The company's first foray into drug development was a small molecule treatment for ulcerative colitis (SGM-1019). [3] [5] [notes 1] [notes 2] The mechanism of SGM-1019 has not been disclosed in detail. [5] Key to the company's business model has been partnerships with large established pharmaceutical companies, including Pfizer and Janssen. [1] Potential competitors to Second Genome include Kaleido Biosciences, Synlogic, Kallyope, Seres Therapeutics, OpenBiome, Rebiotix, Evelo Therapeutics, [2] and Vedanta Biosciences. [3]

Second Genome was founded in 2010 by Corey Goodman, a venture capitalist and former Pfizer executive, [3] and Todd DeSantis, the company's vice president for informatics as of 2019. [6] As of 2013, the company had entered into an ulcerative colitis research agreement with Janssen, [7] the financial arrangement and outcome of which remains to be determined. The company had a headcount of 18 employees as of 2014, [1] which had increased to 25 by 2016. [3] Startup financing was obtained through a Series A round which raised US$11.5 million. [1] A Series B round of funding raised US$42.6 million in 2016. [3] By 2016, the company had established a DNA sequencing service aimed at microbial samples, which provided revenue to supplement venture capital infusions. [3] As of 2019, the company had secured a two-year SBIR grant in collaboration with Oregon State University, aimed at studying microbiome metabolites from people suffering from nervous system disorders, in particular autism. [6]

As of 2016, the company's president and chief executive officer was Peter DiLaura. [1] [3]

Notes

  1. Searches in clinicaltrials.gov on 3 August 2017 did not reveal information about trials sponsored by Second Genome or using the therapeutic SGM-1019.
  2. Timmerman 2016 refers to indication being ulcerative colitis; Lash 2015 refers to indication being Crohn's disease.

Related Research Articles

<span class="mw-page-title-main">Human microbiome</span> Microorganisms in or on human skin and biofluids

The human microbiome is the aggregate of all microbiota that reside on or within human tissues and biofluids along with the corresponding anatomical sites in which they reside, including the skin, mammary glands, seminal fluid, uterus, ovarian follicles, lung, saliva, oral mucosa, conjunctiva, biliary tract, and gastrointestinal tract. Types of human microbiota include bacteria, archaea, fungi, protists, and viruses. Though micro-animals can also live on the human body, they are typically excluded from this definition. In the context of genomics, the term human microbiome is sometimes used to refer to the collective genomes of resident microorganisms; however, the term human metagenome has the same meaning.

<span class="mw-page-title-main">Infliximab</span> Pharmaceutical drug

Infliximab, a chimeric monoclonal antibody, sold under the brand name Remicade among others, is a medication used to treat a number of autoimmune diseases. This includes Crohn's disease, ulcerative colitis, rheumatoid arthritis, ankylosing spondylitis, psoriasis, psoriatic arthritis, and Behçet's disease. It is given by slow injection into a vein, typically at six- to eight-week intervals.

<span class="mw-page-title-main">Inflammatory bowel disease</span> Medical condition

Inflammatory bowel disease (IBD) is a group of inflammatory conditions of the colon and small intestine, Crohn's disease and ulcerative colitis (UC) being the principal types. Crohn's disease affects the small intestine and large intestine, as well as the mouth, esophagus, stomach and the anus, whereas ulcerative colitis primarily affects the colon and the rectum.

<span class="mw-page-title-main">Colitis</span> Inflammation of the colon (large intestine)

Colitis is swelling or inflammation of the large intestine (colon). Colitis may be acute and self-limited or long-term. It broadly fits into the category of digestive diseases.

<span class="mw-page-title-main">Clostridia</span> Class of bacteria

The Clostridia are a highly polyphyletic class of Bacillota, including Clostridium and other similar genera. They are distinguished from the Bacilli by lacking aerobic respiration. They are obligate anaerobes and oxygen is toxic to them. Species of the class Clostridia are often but not always Gram-positive and have the ability to form spores. Studies show they are not a monophyletic group, and their relationships are not entirely certain. Currently, most are placed in a single order called Clostridiales, but this is not a natural group and is likely to be redefined in the future.

<span class="mw-page-title-main">Gut microbiota</span> Community of microorganisms in the gut

Gut microbiota, gut microbiome, or gut flora, are the microorganisms, including bacteria, archaea, fungi, and viruses, that live in the digestive tracts of animals. The gastrointestinal metagenome is the aggregate of all the genomes of the gut microbiota. The gut is the main location of the human microbiome. The gut microbiota has broad impacts, including effects on colonization, resistance to pathogens, maintaining the intestinal epithelium, metabolizing dietary and pharmaceutical compounds, controlling immune function, and even behavior through the gut–brain axis.

<span class="mw-page-title-main">Fecal microbiota transplant</span> Process of transplantation of fecal bacteria from a healthy individual into a recipient

Fecal microbiota transplant (FMT), also known as a stool transplant, is the process of transferring fecal bacteria and other microbes from a healthy individual into another individual. FMT is an effective treatment for Clostridioides difficile infection (CDI). For recurrent CDI, FMT is more effective than vancomycin alone, and may improve the outcome after the first index infection.

Dysbiosis is characterized by a disruption to the microbiome resulting in an imbalance in the microbiota, changes in their functional composition and metabolic activities, or a shift in their local distribution. For example, a part of the human microbiota such as the skin flora, gut flora, or vaginal flora, can become deranged, with normally dominating species underrepresented and normally outcompeted or contained species increasing to fill the void. Dysbiosis is most commonly reported as a condition in the gastrointestinal tract.

Ustekinumab, sold under the brand name Stelara, is a monoclonal antibody medication developed by Janssen Pharmaceuticals, for the treatment of Crohn's disease, ulcerative colitis, plaque psoriasis and psoriatic arthritis, targeting both IL-12 and IL-23.

The Crohn's & Colitis Foundation (CCF) is a volunteer-driven non-profit organization in the US that works to fund research for cures for Crohn's disease and ulcerative colitis and to improve the quality of life of people affected by these digestive diseases. Founded by Shelby Modell and Irwin M. Rosenthal, and formerly known as National Foundation for Ileitis and Colitis and Crohn's and Colitis Foundation of America, it was incorporated on December 17, 1965. CCF has more than 50,000 members, served by the national headquarters, as well as over 40 chapters nationwide.

<span class="mw-page-title-main">Human Microbiome Project</span> Former research initiative

The Human Microbiome Project (HMP) was a United States National Institutes of Health (NIH) research initiative to improve understanding of the microbiota involved in human health and disease. Launched in 2007, the first phase (HMP1) focused on identifying and characterizing human microbiota. The second phase, known as the Integrative Human Microbiome Project (iHMP) launched in 2014 with the aim of generating resources to characterize the microbiome and elucidating the roles of microbes in health and disease states. The program received $170 million in funding by the NIH Common Fund from 2007 to 2016.

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Sarkis Mazmanian is an American medical microbiologist who has served as a professor at the California Institute of Technology since 2006. He is currently the Luis & Nelly Soux Professor of Microbiology in the Division of Biology and Biological Engineering, and a board member of Seed. Prior to this, Mazmanian was affiliated with Harvard Medical School and the University of Chicago. In 2012, Mazmanian was awarded a MacArthur Fellowship for his pioneering work on the human microbiome.

<span class="mw-page-title-main">Pharmacomicrobiomics</span>

Pharmacomicrobiomics, proposed by Prof. Marco Candela for the ERC-2009-StG project call, and publicly coined for the first time in 2010 by Rizkallah et al., is defined as the effect of microbiome variations on drug disposition, action, and toxicity. Pharmacomicrobiomics is concerned with the interaction between xenobiotics, or foreign compounds, and the gut microbiome. It is estimated that over 100 trillion prokaryotes representing more than 1000 species reside in the gut. Within the gut, microbes help modulate developmental, immunological and nutrition host functions. The aggregate genome of microbes extends the metabolic capabilities of humans, allowing them to capture nutrients from diverse sources. Namely, through the secretion of enzymes that assist in the metabolism of chemicals foreign to the body, modification of liver and intestinal enzymes, and modulation of the expression of human metabolic genes, microbes can significantly impact the ingestion of xenobiotics.

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Andre Franke, born on 16 October 1978, is a geneticist, academic, and university professor. He is a Full W3 Professor of Molecular Medicine at the Christian-Albrechts-University of Kiel, and a managing director at the Institute of Clinical Molecular Biology.

<span class="mw-page-title-main">Seed (company)</span>

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Phocaeicola vulgatus,, is a mutualistic anaerobic Gram negative rod bacteria commonly found in the human gut microbiome and isolated from feces. P. vulgatus has medical relevance and has been notable in scientific research due to its production of fatty acids, potential use as a probiotic, and associations with protecting against and worsening some inflammatory diseases. Due to the difficulties in culturing anaerobic bacteria, P. vulgatus is still highly uncharacterised so efforts are being made to make use of multi-omic approaches to investigate the human gut microbiome more thoroughly in hopes to fully understand the role of this species in the development of and protection against diseases, as well as its potential uses in medicine and research. Generally, P. vulgatus is considered as a beneficial bacteria that contributes to digestion and a balanced microbiome, but it has been known to cause opportunistic infections and induce or worsen inflammatory responses. Due to its abundance in the microbiome, some researchers are investigating these species in hopes that it will be a suitable model organism for gut microbiome research, like Bacteroides thetaiotaomicron.

References

  1. 1 2 3 4 5 6 Koberstein, Wayne (July 2014). "Second Geome" . Companies To Watch. Life Science Leader. Jameson Publishing. 6 (7): 14.
  2. 1 2 Jacobson, Don (19 July 2017). "Mayo Continues Venture Funding of Gut Microbiome Companies with Latest Stake". Twin Cities Business. Minnesota, United States: MSP Communications. Retrieved 4 August 2017. Second Genome's product is essentially a platform that combines genomics technologies, computational biology, and phenotypic screening which allows researchers to develop drugs....
  3. 1 2 3 4 5 6 7 8 Timmerman, Luke (20 April 2016). "Pfizer, Roche Embrace The Microbiome, Leading $43M Bet On Second Genome". Forbes.
  4. Shukla, Triveni P. (2014). Our Genes, Our Foods, Our Choices. Bloomington, Indiana, United States: Author House. p. 89. ISBN   9781496928580. OCLC   890626454. One hundred trillion bacteria in our colon and their genes, our second genome, matter to our immunity and sustainable health. --Triveni P. Shukla
  5. 1 2 Lash, Alex (12 January 2015). "Second Genome Has Begun First Drug Trial Based on Microbiome Secrets". Xconomy. Retrieved 4 August 2017.
  6. 1 2 Lundeberg, Steve (25 May 2019). "OSU part of $1.94 million grant to study connection between autism, microbiome". The World. Oregon, United States: Lee Enterprises. p. A12. Retrieved 12 February 2021 via Newspapers.com.
  7. Sell, David (9 June 2013). "Large, small drug firms join for profitable results". The Philadelphia Inquirer. Vol. 185, no. 9. Interstate General Media. p. D4. Retrieved 12 February 2021 via Newspapers.com.